BEUDAMED
    38 results · 35ms · Sources: EU EUDAMED, US FDA

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    Drug Relief v1

    FDA 510(k)
    FDA Class 2 ·Neurology

    Adler Instrument Company

    FDA UDI
    Adler, Inc.·00810123209132·Castroviejo Needle Holder TC Straight, Serrated...

    NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    IND DRUG HOME MULTI-PANEL TEST (2-5) IND MORPHINE HOME TEST

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 16, 2025

    BD LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 27, 2024

    2520274-2014-00851

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQV·February 25, 2014

    2520274-2014-00854

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDN·February 26, 2014

    JAG PRECURSOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZB·November 5, 2008

    POLY-L-LACTIC ACID (POLY-L-LACTIC ACID)

    FDA Adverse Event
    Injury ·AVENTIS PHARMA GRUPPO S.R.L.·Product code LMH·August 18, 2011

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 11, 2013

    BD BACTEC¿ PLUS AEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·April 18, 2024

    BD BACTEC¿ PLUS AEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·April 18, 2024

    1823260-2017-01875

    FDA Adverse Event
    Malfunction ·August 31, 2017

    2520274-2014-00857

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQV·February 26, 2014

    2520274-2014-00853

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 26, 2014

    2520274-2014-00856

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDN·February 26, 2014

    UNKNOWN IMPLANTABLE DEEP BRAIN STIMULATION NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 14, 2013

    2520274-2014-00852

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDN·February 26, 2014

    2520274-2014-00845

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDN·February 25, 2014